Structure of PDB 4x36 Chain A Binding Site BS01
Receptor Information
>4x36 Chain A (length=318) Species:
170187
(Streptococcus pneumoniae TIGR4) [
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MEINVSKLRTDLPQVGVQPYRQVHAHSTGNPHSTVQNEADYHWRKDPELG
FFSHIVGNGCIMQVGPVDNGAWDVGGGWNAETYAAVELIESHSTKEEFMT
DYRLYIELLRNLADEAGLPKTLDTGSLAGIKTHEYCTNNQPNNHSDHVDP
YPYLAKWGISREQFKHDIENGLTIETGWQKNDTGYWYVHSDGSYPKDKFE
KINGTWYYFDSSGYMLADRWRKHTDGNWYWFDNSGEMATGWKKIADKWYY
FNEEGAMKTGWVKYKDTWYYLDAKEGAMVSNAFIQSADGTGWYYLKPDGT
LADKPEFTVEPDGLITVK
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
4x36 Chain A Residue 407 [
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Receptor-Ligand Complex Structure
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PDB
4x36
Full-length structure of the major autolysin LytA.
Resolution
2.101 Å
Binding residue
(original residue number in PDB)
H26 H133 D149
Binding residue
(residue number reindexed from 1)
H26 H133 D149
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N69 A71 K165
Catalytic site (residue number reindexed from 1)
N69 A71 K165
Enzyme Commision number
3.5.1.28
: N-acetylmuramoyl-L-alanine amidase.
Gene Ontology
Molecular Function
GO:0008745
N-acetylmuramoyl-L-alanine amidase activity
GO:0016787
hydrolase activity
Biological Process
GO:0009253
peptidoglycan catabolic process
GO:0030420
establishment of competence for transformation
GO:0030435
sporulation resulting in formation of a cellular spore
GO:0071555
cell wall organization
Cellular Component
GO:0005576
extracellular region
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4x36
,
PDBe:4x36
,
PDBj:4x36
PDBsum
4x36
PubMed
26057677
UniProt
P06653
|ALYS_STRPN Autolysin (Gene Name=lytA)
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